The relative affinities of Cd,Ni and Zn for different soil clay fractions and goethite

Cadmium, Ni and Zn ions in aqueous solution were allowed to react with clay fractions (< 2 μm) separated from soils with a wide range of mineralogical composition and properties. Sorbed metals were separated into two components, termed specifically and non-specifically bound, by a controlled washing procedure using 10^?2M Ca(NO₃)₂.Sorption reactions were characterized by Δ pH₅₀ values, by shapes of adsorption curves, and by measuring separation factors and distribution coefficients under prescribed conditions. Three reaction types were identified, viz., (i) those associated with soil adsorbing surfaces dominated by iron oxides; these appear to be controlled by mechanisms which involve metal-ion hydrolysis and result accordingly in relative sorption affinities of Zn > Ni > Cd; (ii) those associated with organic surfaces for which metal-ion hydrolysis was of little significance and little difference in metal-ion affinity was evident; at lower pH-values, Cd and Ni were somewhat preferred over Zn, with the converse at higher pH-values; (iii) those associated with 2:1 layer lattice silicates which exhibit greater preference for Zn, i.e., Zn >> Ni, Cd and higher affinities for each metal at lower pH-values (< 5) than is shown by clays dominated by iron oxides. There was also evidence of greater relative affinity for Ni shown by clay fractions dominated by fine kaolinites when compared with other clays.This investigation has shown that a range of sorption processes are involved in reactions of heavy metals with soils. We caution against undue emphasis on any particular sorption process in developing theoretical sorption models as a basis of understanding and solving problems connected with pollution and plant nutrition; we also stress the need for studies with colloids separated from soils in conjunction with those using synthetic adsorbents as models for soil constituents.     

Competitive Effect of Copper,Zinc, Cadmium and Nickel on Ion Adsorption and Desorption by Soil Clays

This study evaluated the effect of competing copper, zinc, cadmium and nickel ions in 0.01 M Ca(NO₃)₂ on heavy metal sorption and desorption by soil clay fractions. Initial Cu addition levels varied from 99 mg kg^-1 to 900 mg kg^-1 and Zn, Cd and Ni levels were 94, 131 and 99 mg kg^-1, respectively. Sorption of Cu conformed to a Freundlich equation. The amounts of metals not displaced by successive 48 h desorption cycles with 0.01 M Ca(NO₃)₂ were considered ‘specifically adsorbed’. Total sorption of Zn and Cd generally decreased in the order: Vertisol > Gleyic Acrisol > Planosol clay. More than 70% of the copper was specifically sorbed. Specific sorption of Zn was depressed by competition with Cu in the three clays investigated. At surface coverages higher than 200 mg Cu per kg of soil clay, zinc sorption in the Planosol and Gleyic Acrisol clays took place at low affinity sites. The exchangeable component of sorbed cadmium accounted for >:60% of the sorption in the Vertisol clay, >70% in the Gleyic Acrisol clay and was almost 100% in the Planosol clay. Nickel was not retained by the Planosol and Gleyic Acrisol clays and was ionexchangeably adsorbed by the Vertisol clay. At the conditions studied, Ni and Cd remain a ready source of pollution hazard.     

Development of an Environmentally Friendly Adsorbent for the Removal of Toxic Heavy Metals from Aqueous Solution

An effective adsorbent for the removal of heavy metals was manufactured by immobilization of jujube powder. The adsorptions of Cd, Zn and Cu from aqueous solutions by jujube complex beads (Type 1 and Type 2) were studied in a batch adsorption system. The adsorption data were fitted well with the Langmuir isotherm models. The adsorption capacities (β) for Cd, Zn and Cu were 4.23, 2.93 and 3.64 mg/g in Type 1 and 1.24, 0.70 and 1.35 mg/g in Type 2 beads. The removal efficiencies of the Type 2 beads, with a larger unit surface area, were lower than those of the Type 1 due to part of the casein or cyclic AMP being destroyed during the drying process of the Type 1. These values for Type 1 beads were higher than those of all other adsorbents for each heavy metal. A comparison of the kinetic models on the overall adsorption rate showed that the adsorption system was best described by pseudo-first-order kinetics. The removal efficiencies of Cd, Zn and Cu exhibited similar tendencies to those observed in the equilibrium tests. This indicates that the jujube complex beads developed in this study can be used as promising adsorbents for the removal of heavy metals from wastewater.     

Verhalten von Schwermetallen in Böden 1. Untersuchungen zur Schwermetallmobilität

Behaviour of heavy metals in soils. 1. Heavy metal mobility 158 soil samples with widely varying composition were analysed for their total, EDTA, DTPA and CaCl₂ extractable contents of Cd, Zn, Mn, Cu and Pb. By means of single and multiple regressions the relations between the different heavy metal fractions and the pH, organic carbon and clay content were considered. The correlations between the total, EDTA and DTPA extractable contents are very close, whereas the CaCl₂ extractable contents are not or only weakly correlated with these fractions. According to these statistical results the former fractions are considered to be the total quantity (total content) and the reactive quantity (EDTA and DTPA extractable contents) of the heavy metals, whereas the CaCl₂ extractable fraction represents the mobile fraction of the heavy metals in soils. The multiple regressions show that the mobile content of heavy metals is closely correlated with each of the quantity fractions and with soil pH. In the same way the proportion of the mobile fraction (in %) of the total, EDTA and DTPA extractable heavy metal content of the soil samples is closely related to the soil pH. Hereby the proportion of the mobile content of the various elements increases in the pH range 6,5 - 3 below element-specific threshold pH values (in brackets) in the order Cd (6,5) > Mn (5,7) > Zn (5,3) > Cu (4,5) > Pb (3,5). In the pH range 6,5 - 7,5 mainly Cu and to a lesser degree also Pb show an increasing mobility due to the influence of soluble organic substances.     

Assessment of Fe,Zn, Cd,Hg, and Pb in the Jordan and Yarmouk River Sediments in Relation to Their Physicochemical Properties and Sequential Extraction Characterization

Forty-six surface sediment samples taken along the beds of boththe Jordan and Yarmouk Rivers were analysed for Pb, Cd, Zn, Fe andHg by atomic absorption spectrophotometer. Extraction techniqueswere used to establish the association of the total concentrations of Pb, Cd, Zn and Fe in the sediment samples withtheir contents in the exchangeable, carbonate, Fe/Mn oxides, organic and residual fractions.In the sediments of the Jordan River the recorded heavy metalsconcentrations were as follow: 8.1 ppm for Pb, 0.63 ppm for Cd, 20.3 ppm for Zn, 6 ppm for Hg and 1265.6 ppm for Fe; whereas in the sediment of Yarmouk River were 8.4 ppm for Pb, 0.67 ppm for Cd, 26.4 ppm for Zn, 6.2 ppm for Hg and 1370 ppmfor Fe. Pb, Cd, Zn, and Fe concentrations in the sediments ofboth rivers reflect the natural background value in shale, whereas Hg is moderately enriched. I-geo (geo-accumulation index) of metals in the sediments under study indicates thatthey are uncontaminated with Pb, Zn and Fe; contaminated tomoderately contaminated with Cd; and strongly contaminated with Hg. Heavy metal content in the sediments were found to be significantly influenced by different physico-chemical parameters. The effect of these physico-chemical parameters canbe arranged in the following order: clay fraction > organicmatter fractions > carbonate fraction > silt fraction. As sequential extraction procedure shows that the total concentration of the heavy metals are largely bound to the residual phase (retained 79.5% of Pb, 38% of Cd, 54.4% of Zn and 51.6% of Fe in Jordan River Sediments; and 88.6% of Pb, 48.2% of Cd, 37.6% of Zn and 59.5% of Fe in the YarmoukRiver sediments). The following sequence of mobility are suggested: Fe > Cd > Zn > Pb in Jordan River sediments, and Fe > Zn > Cd > Pb. in Yarmouk River sediments.     

Comparison of Heavy Metal Adsorptions by Thai Kaolin and Ballclay

The adsorption characteristics of heavy metals: cadmium(II), chromium(III), copper(II), nickel(II), lead(II), and zinc(II) ions by kaolin (kaolinite) and ballclay (illite) from Thailand were studied. This research was focussed on the pH, adsorption isotherms of single-metal solutions at 30–60 °C by batch experiments, and on ion selectivityin mixed and binary combination solutions. It was found that, except Ni, metal adsorption increased with increased pH of the solutions and their adsorption followed both Langmuir and Freundlich isotherms. Adsorption of metals in the mixture solutions by kaolin was: Cr > Zn > Cu ≈ Cd ≈ Ni > Pb, and for ballclay was: Cr > Zn > Cu > Cd ≈ Pb > Ni. The adsorption of metals was endothermic, with the exception of Cd, Pb and Zn for kaolin, Cu and Zn for ballclay. Kaolin and ballclay exhibited relatively hard Lewis base adsorption site. The presence of other metals may reduce or promote the adsorption of heavy metals. The presence of Cr³⁺ induced the greatest reduction of metal adsorptiononto kaolin, as did the presence of Cu²⁺ for ballclay.     

Heavy Metal Release from Some Industrial Wastes: Influence of Organic and Inorganic Acids, Clay Minerals, and Nanoparticles

Knowledge about heavy metal release from industrial solid wastes(ISWs) is crucial for better management of their environmental risks. This study was conducted to investigate the effect of organic and inorganic acids, clay minerals, and nanoparticles(NPs) on the release of heavy metals from sugar factory waste, ceramic factory waste, leather factory waste, and stone cutting waste. The influence of the extractants on heavy metal release from these ISWs was in the following descending order: citric acid oxalic acid nitric acid≥ sulfuric acid Ca Cl2. Addition of clay minerals and NPs as adsorbents decreased heavy metal release, which was significantly lower in NP-treated wastes than in the clay mineral-treated wastes. On the other hand, the presence of organic and inorganic acids increased heavy metal adsorption by NPs and clay minerals. These results suggest that NPs can be applied successfully in waste remediation,and organic and inorganic acids play an important role in the removal of heavy metals from the studied adsorbents.     

Pollution and Ecological Risk Assessment of Heavy Metals in Farmland Soils in Yanqi County,Xinjiang, Northwest China

A total of 50 farmland soil samples were collected from the Yanqi County, Xinjiang, China, and the concentrations of eight heavy metal elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn) were determined by standard methods. The spatial distribution, pollution level and ecological risk status of heavy metals were analyzed based on GIS technology, the Geo-accumulation Index (Igeo), the Pollution Load Index (PLI) and the Potential Ecological Risk Index (RI). Results indicated that: (1) The average contents of Cd, Cr, Ni, Pb, and Zn of farmland soils exceeded the background values of irrigation soils in Xinjiang by 1.5, 1.40, 1.33, 2.63, and 4.92 times, respectively. Cd showed a no-pollution level, Zn showed a partially moderate pollution level, Pb showed a slight pollution level, and Cr, Cu, As, Mn, and Ni showed no-pollution level, compared to the classification standard. The PLI values of heavy metal elements of farmland soils varied from 0.83 to 1.89, with an average value of 1.29, at the moderate pollution level. (2) The Individual Potential Ecological Risk Index for heavy metals in the study area was ranked in the order of: As > Ni > Cu > Cd > Pb > Cr> Zn. The RI values of heavy metals of farmland soils varied from 3.45 to 11.34, with an average value of 6.13, at the low ecological risk level. (3) Cu and Mn of farmland soils were mainly originated from the soil parent material and topography of the study area. As, Cd, Ni and Pb were mainly originated from human activities, and Cr and Zn may originated from both natural and anthropogenic factors in the study area.     

The transfer of heavy metals to barley plants from soils amended with sewage sludge with different heavy metal burdens

Purpose

Our main aim objective was to evaluate the transfer of Cd, Cr, Cu, Ni, Pb and Zn to barley (Hordeum vulgare) grown in various soils previously amended with two sewage sludges containing different concentrations of heavy metals. This allowed us to examine the transfer of heavv metals to barley roots and shoots and the occurrence of restriction mechanisms as function of soil type and for different heavy metal concentration scenarios.

Material and methods

A greenhouse experiment was performed to evaluate the transfer of heavy metals to barley grown in 36 agricultural soils from different parts of Spain previously amended with a single dose (equivalent to 50 t dry weight ha^?1) of two sewage sludges with contrasting levels of heavy metals (common and spiked sludge: CS and SS).

Results and discussion

In soils amended with CS, heavy metals were transferred to roots in the order (mean values of the bio-concentration ratio in roots, BCF_Roots, in brackets): Cu (2.4)?~?Ni (2.3)?>?Cd (2.1)?>?Zn (1.8)?>?Cr (0.7)?~?Pb (0.6); similar values were found for the soils amended with SS. The mean values of the soil-to-shoot ratio were: Cd (0.44)?~?Zn (0.39)?~?Cu (0.39)?>?Cr (0.20)?>?Ni (0.09)?>?Pb (0.01) for CS-amended soils; Zn (0.24)?>?Cu (0.15)?~?Cd (0.14)?>?Ni (0.05)?~?Cr (0.03)?>?Pb (0.006) for SS-amended soils. Heavy metals were transferred from roots to shoots in the following order (mean values of the ratio concentration of heavy metals in shoots to roots in brackets): Cr (0.33)?>?Zn (0.24)?~?Cd (0.22)?>?Cu (0.19)?>?Ni (0.04)?>?Pb (0.02) for CS-amended soils; Zn (0.14)?>?Cd (0.09)?~?Cu (0.08)?>?Cr (0.05)?>?Ni (0.02)?~?Pb (0.010) for SS-amended soils.

Conclusions

Soils weakly restricted the mobility of heavy metals to roots, plant physiology restricted the transfer of heavy metals from roots to shoots, observing further restriction at high heavy metal loadings, and the transfer of Cd, Cu and Zn from soils to shoots was greater than for Cr, Ni and Pb. Stepwise multiple linear regressions revealed that soils with high sand content allowed greater soil-plant transfer of Cr, Cu, Pb and Zn. For Cd and Ni, soils with low pH and soil organic C, respectively, posed the highest risk.     

Evaluation of Green Waste and Popular Twigs Biochar Produced at Low and High Pyrolytic Temperature for Efficient Removal of Metals from Water

Biomass-derived biochar is considered as a promising heavy metal adsorbent, due to its favorable physicochemical properties, from aqueous solution as compared with other adsorbents. However, there is a limited number of studies on the effects of biochar produced from different feedstocks and pyrolytic temperatures on metal removal from metal-contaminated water. So in this study, the removal of the most prevalent heavy metals [(lead (Pb(II)), cadmium (Cd), and chromium (Cr)] by green waste biochar (GWB) and popular twigs biochar (PTB), produced at different pyrolytic temperatures, i.e., low 350 and high 650 °C, has been investigated, following the determination of physical and chemical properties of biochar. The efficiency of heavy metals removal of biochar was studied at different concentrations of heavy metals (10 and 100 μg mL^?1), biochar types and treatment duration (3, 6, 9, and 12 h) at isothermic condition of aqueous solution. Results revealed that both feedstock type and pyrolytic temperature to produce biochar significantly affected its metal sorption capacity. The maximum sorption capacities of all three metals, i.e., Pb (II), Cd, and Cr were determined in the GWB produced at low pyrolytic temperature 350 °C after 9 h of treatment duration at both high and low metal concentrations. This highest sorption capacity of all metals by low pyrolytic temperature produced GWB was due to its better physicochemical properties especially high surface area, cation exchange capacity, and oxygen-containing functional groups as compared with woody feedstock based high pyrolytic temperature produced PTB. Conclusively, low pyrolytic temperature produced GWB was evaluated as a potential adsorbent to efficiently reduced heavy metal concentration in metal-contaminated water.     

Soil cadmium stabilization using an Iranian natural zeolite

In recent years, natural substances such as zeolite have been used to absorb heavy metals in soil in an attempt to decrease their availability to plants. Compared to other techniques, the use of zeolite is fast, clean, and inexpensive. This research was carried out to investigate the effects of an Iranian natural zeolite (clinoptilolite) on stabilizing Cd-contaminated soil treated with 0.01 M CaCl₂ leaching solution. Zeolite from Firoozkouh (Tehran Province) was added to four soils from Gilan province, northern Iran. The stabilization of Cd in soils mixed with zeolite was measured in both column and batch experiments. The results from the batch experiment showed that application of zeolite to soil reduced Cd leaching in all the contaminated soils. When more zeolite was added to soil, lower Cd concentrations were detected in the leaching solution. When 15% zeolite was applied, Cd concentration in the leachate decreased to below 0.1 mg l^− 1. Cadmium depth analysis showed little migration of Cd in sand and clay textures with no zeolite addition and after adding 15 and 75 pore volumes of leaching solution, the remaining Cd levels were 12% and 35% of the original Cd concentration, respectively. However, these values for 9% zeolite treatments were 97% and 99%, respectively. The higher cation exchange capacity of the zeolite/soil mixture and the higher pH levels were responsible for stabilizing Cd in these soils. The effect of preventing heavy metals from leaching was found to be more pronounced when zeolite was applied to clay soils.     

Heavy metals in the soil–plant system of the Don River estuarine region and the Taganrog Bay coast

Purpose

The aim of this work was to study the level and degree of mobility of heavy metals in the soil–plant system and to perform bioindication observations in the Don River estuarine region and the Russian sector of the Taganrog Bay coast.

Materials and methods

The objects of the study included samples of zonal soils (chernozem) and intrazonal soils (alluvial meadow and alluvial-stratified soils, Solonchak, sandy primitive soil) from monitoring stations of the Don river estuarine region and the Taganrog Bay coast, as well as their higher plants: Phragmites australis Cav., Typha angustifolia L., Carex riparia Curtis, Cichorium intybus L., Bolboschoenus maritimus L. Palla, and Rumex confertus Willd. The total concentrations of Mn, Ni, Cd, Cu, Zn, Pb, and Cr in the soils were determined by X-ray fluorescent scanning spectrometer. The concentration of heavy metal mobile forms exchangeable, complex compounds, and acid-soluble metal were extracted using the following reagents: 1 N NH₄Ac, pH 4.8; 1 % EDTA in NH₄Ac, pH 4.8; 1 N HCl, respectively. Heavy metals in plants were prepared for analysis by dry combustion at 450 °C. The heavy metal concentration in extracts from plants and soils was determined by AAS.

Results and discussion

The total contents of heavy metals in the soil may be described with a successively decreasing series: Mn?>?Cr?>?Zn?>?Ni?>?Cu?>?Pb?>?As?>?Cd. The total concentrations of As, Cd, and Zn in the soil exceed the maximum permissible concentrations levels. Contamination of alluvial soils in the estuarine zone with mobile Сu, Zn, Pb, and Cd has been revealed, which is confirmed by the high bioavailability of Cu and Zn and, to a lesser degree, Cd and Pb accumulating in the tissues of macrophytic plants. Data on the translocation of elements to plant organs have showed their predominant accumulation in the roots. Bioindication by the morphofunctional parameters of macrophytic plants (with a Typha L. species as an example) can be used for revealing the existence of impact zones with elevated contents of metals in aquatic ecosystems.

Conclusions

The results revealed that increased content of Zn, Pb, Cu, Ni, and As in soil have anthropogenic sources. The high content of Cr in the soils is related to the lithogenic factor and, hence, has a natural source.

     

Effect of Clay Minerals on Immobilization of Heavy Metals and Microbial Activity in a Sewage Sludge-Contaminated Soil (8 pp)

Background   Aims, and Scope. Reducing heavy metal solubility and bioavailability in contaminated area without removing them from the soil is one of the common practices in decreasing the negative impacts on the environment and improving the soil quality. Therefore, our aim was to study the effect of clay minerals: Na-bentonite, Ca-bentonite, and zeolite applied to a contaminated soil on immobilization of heavy metals, as well as on some soil parameters related with microbial activity. Methods   A soil derived from sewage sludge was incubated with clay minerals of either Na-bentonite, Ca-bentonite, or zeolite for 111 days (d). During the incubation experiment, concentrations of water soluble Zn, Cd, Cu, and Ni were measured after extraction of 2 g air-dry soil with 50 ml of H2O for 2 h. After the water extraction, the soil sediment was extracted with 50 ml of 1 M NH4NO3 for 2 h to estimate the exchangeable amounts of heavy metals. Furthermore, soil microbial respiration, microbial biomass C, Corg mineralization, metabolic quotient (qCO2), and inorganic N were also investigated. Results and Discussion   Water extractable and exchangeable forms of heavy metals were changed by incubation and addition of clay minerals. Incubation of soil without addition of clay minerals (control) increased water extractable Cu by 12, 24 and 3.8% of initial content after 21, 62, and 111 d of incubation, respectively. The water extractable Zn decreased by 9% during 62 d of incubation and it tended to increase by 14% at the end of the incubation, as compared with the initial soil. Water extractable Cd decreased by 71, 66 and 33% of initial content, and Ni decreased by 54, 70, and 58%, after 21, 62, and 111 d of incubation, respectively. During the incubation experiment, the exchangeable form of all tested metals was decreased by incubation. The addition of clay minerals led to a significant decrease in water soluble and exchangeable forms of heavy metals during the incubation experiment, resulting in low metal extractability. The reduction in metal extractability was greater due to the addition of Na-bentonite or Ca-bentonite than that due to the addition of zeolite. During the first 3 weeks after addition of clay minerals, the studied biological parameters were not affected. However, as incubation progressed, the addition of Na- or Ca- bentonite led to a significant increase in soil respiration, microbial biomass C, Corg mineralization, and inorganic N; and a significant decrease in qCO2. This result is explained by sorption of heavy metals on Na-bentonite and Ca-bentonite and strong reduction of their toxicity. Conclusions   Our results clearly show that the addition of clay minerals, especially of Na-bentonite and Ca-bentonite, decreased the extractability of four metals during incubation. The decreased metal extractability was accompanied by an increase of soil respiration, Corg mineralization, microbial biomass C, and inorganic N and a decrease of metabolic quotient (qCO2), showing positive effect of clay mineral addition on soil biological parameters. Recommendations and Outlook   The use of Na-bentonite and Ca-bentonite is promising tool for reduction the extractability and possible toxicity of heavy metals in sewage sludge-contaminated soil. Therefore, the soils polluted with heavy metals may be ameliorated by addition of clay minerals, especially Na-bentonite and Ca-bentonite.     

Heavy‐Metal Contamination of Soil and Vegetables in Wastewater‐Irrigated Agricultural Soil in a Suburban Area of Hanoi,Vietnam

The To Lich and Kim Nguu Rivers, laden with untreated waste from industrial sources, serve as sources of water for irrigating vegetable farms. The purposes of this study were to identify the impact of wastewater irrigation on the level of heavy metals in the soils and vegetables and to predict their potential mobility and bioavailability. Soil samples were collected from different distances from the canal. The average concentrations of the heavy metals in the soil were in the order zinc (Zn; 204 mg kg^?1) > copper (Cu; 196 mg kg^?1) > chromium (Cr; 175 mg kg^?1) > lead (Pb; 131 mg kg^?1) > nickel (Ni; 60 mg kg^?1) > cadmium (Cd; 4 mg kg^?1). The concentrations of all heavy metals in the study site were much greater than the background level in that area and exceeded the permissible levels of the Vietnamese standards for Cd, Cu, and Pb. The concentrations of Zn, Ni, and Pb in the surface soil decreased with distance from the canal. The results of selective sequential extraction indicated that dominant fractions were oxide, organic, and residual for Ni, Pb, and Zn; organic and oxide for Cr; oxide for Cd; and organic for Cu. Leaching tests for water and acid indicated that the ratio of leached metal concentration to total metal concentration in the soil decreased in the order of Cd > Ni > Cr > Pb > Cu > Zn and in the order of Cd > Ni > Cr > Zn > Cu > Pb for the ethylenediaminetetraaceitc acid (EDTA) treatment. The EDTA treatment gave greater leachability than other treatments for most metal types. By leaching with water and acid, all heavy metals were fully released from the exchangeable fraction, and some heavy metals were fully released from carbonate and oxide fractions. The concentrations of Cd, Cr, Cu, Ni, Pb, and Zn in the vegetables exceeded the Vietnamese standards. The transfer coefficients for the metals were in the order of Zn > Ni > Cu > Cd = Cr > Pb.     

Effect of aging process on the fractionation of heavy metals in some calcareous soils of Iran

This study was conducted to investigate the effect of time on lead (Pb), zinc (Zn), cadmium (Cd) and copper (Cu) availability in some calcareous soils of Iran. Heavy metals were added to soils at the rate of 500 mg kg^? 1 of Pb, Zn, and Cu and 8 mg kg^? 1 of Cd as chloride. The samples were incubated for 3 h, 1, 3, 7, 14, 21, and 28 days at 25 °C and constant moisture. After incubation, metals in amended and control soils were fractionated by the sequential extraction procedure. There were changes in the proportional distribution of heavy metals in all five studied soils during 28 days of incubation with spiked heavy metals. In general the proportions of heavy metals associated with the most weakly bound fraction (EXCH) tended to decrease, with corresponding increases in the other five more strongly binding fractions during the incubation. The distribution of added heavy metals into different solid phase fractions appears to be consisted of two phases involving the initial rapid retention followed by a slow continuous retention. Three kinetic equations were used to fit the experimental data. The parabolic equation fits well the data used in this work. The transformation rate of EXCH fraction for soils was estimated by parabolic equation for above incubation periods. There were differences in the rates at which redistribution took place between soils and heavy metals. The constant b in parabolic equation was defined as the transformation rate, which were in the order Cu > Zn ≥ Pb ? Cd. The higher proportions of EXCH fraction of spiked Cd in these calcareous soils indicates its higher potential of downward leaching and runoff transport especially at the early stage of pollution.     

Assessment of Heavy Metals in Spinach (Spinacia oleracea L.) Grown in Sewage Sludge–Amended Soil

The assessment of heavy metals in spinach (Spinacia oleracea) grown in sewage sludge–amended soil was investigated. The results revealed that sewage sludge significantly (P < 0.01) increased the nutrients and heavy metals such as cadmium (Cd), chromium (Cr), copper (Cu), manganese (Mn), and zinc (Zn) in the soil. The contents of metals were found to be below the maximum levels permitted for soils in India. The most agronomic performance and biochemical components of S. oleracea were found at 50% concentrations of sewage sludge in both seasons. The contents of Cd, Cr, Cu, Mn, and Zn in S. oleracea were increased from 5% to 100% concentrations of sewage sludge in both seasons. The order of contamination factor (Cf) of different heavy metals was Mn > Cd > Cr > Zn > Cu for soil and Cr > Cd > Mn > Zn > Cu for S. oleracea plants after application of sewage sludge. Therefore, use of sewage sludge increased concentrations of heavy metals in soil and S. oleracea.     

Heavy Metal Pollution in Air-Water-Soil-Plant System of Zhuzhou City,Hunan Province,China

The sources, distribution and mobility of heavy metals in Zhuzhou City, Hunan Province, China were systematically studied based on environmental monitoring data and random sampling from fields and markets. The significant positive correlations between some pairs of heavy metals (total Cd–Hg, total Cu–Pb) within the Zhuzhou section of the Xiang River may indicate that they are coming from the same pollution sources with similar pollution channels and removal patterns in the water bodies. Heavy metals from wastewater partly settled in the sediment after entering the Xiang River, which caused an inconsistent change in heavy metal concentrations over time in the middle and lower parts of the Xiang River. There was no significant difference in total Pb and Zn in topsoil between years in the period 1990–1997, which showed the balance between input and output. Heavy metals accumulated mainly in the topsoil with little downward movement. Heavy metals in the vegetables and rice were higher than the edible standard and background value to some degree with minor exceptions. The maximum heavy metal level observed divided by the acceptable level was in the order of Cd > Pb > Cu > Zn. Significant positive correlations were only found between cabbage uptake and total soil content for Hg, Pb and Cd, with no significant correlationfor the other elements. The plant uptake of a heavy metal was somewhat influenced by the co-existence of other elements.     

长江干流沿江地区土壤重金属的分布、来源及潜在生态风险

为掌握长江干流沿江地区土壤重金属状况,开展土壤表层样品采集和重金属空间分布研究,使用PMF（positive matrix factorization）模型解析土壤重金属来源,并选取地累积和潜在生态风险等方法,评估重金属的污染状况和生态风险。结果表明：1）土壤重金属的积累程度不同,As、Cd和Cu的超标率高,污染明显。Cd和Cu的变异系数高于1.0,分布不匀,受某些污染源的影响显著。2）各重金属含量呈现条带状的空间格局,在多个地区出现高值,土壤环境质量受到人类活动的负面影响。3）土壤重金属积累主要来源于自然、工业排放、交通运输和农业生产,贡献率分别为36.65%、28.48%、20.07%和14.80%。其中Cd与工业活动有关,Pb和Zn来自交通排放,Cr和Ni与自然源密切相关,As和Cu来源于农业生产。4）Cd的污染程度最高,81.88%的点位达到轻度污染。40%以上的点位受到As、Cu、Ni和Pb污染。75%以上点位的Cr和Zn含量较低,污染程度不高。单项生态风险指数的均值从大到小依次为：Cd、As、Ni、Cu、Pb、Zn、Cr。综合生态风险指数均值为63.17,处于轻微风险水平。该研究作为土壤生态调查的核心,可为土壤环境管理和重金属污染修复提供科学依据。     

Mikrosondenuntersuchungen an unterschiedlich stark mit Schwermetallen belasteten Böden. 2. Gehalte an Schwermetallen und anderen Elementen in Huminstoffaggregationen,Streustoffen und Holzkohlepartikeln

Electron microprobe studies on soil samples with varying heavy metal contamination. 2. Contents of heavy metals and other elements in aggregations of humic substances, litter residues and charcoal particles EMA point analysis show that the organic matter constituents of heavy metal contaminated soils are highly enriched with heavy metals. The maximal trace element accumulation were for Cu up to 13,000 mg/kg, for Zn up to 48,000 mg/kg, for Cd up to 2,100 mg/kg and for Pb up to 193,000 mg/kg. The affinity for the accumulation of the different heavy metals in aggregations of humic substances can be described by the sequence Cu > Pb ? Cd > Zn ? Ni > Co. In very strongly acidified humic top soil horizons the Pb and Cd accumulation in the organic matter constituents is in competition with the accumulation in Fe and Mn oxides. The heavy metal contents (especially of Cu) of the organic matter are often correlated with the content of organically bound calcium. The EMA results also show that high heavy metal amounts occur in combination with Ca-accumulations in the epidermis and the outer bark parenchym of decayed roots. EMA point analysis of the interior of fungus sclerotias show that sclerotias can contain high amounts of heavy metals, in particular lead (up to 49,700 mg Pb/kg). From statistical results of EMA point analysis follows that lead and other heavy metals attached to humic substances are not only bound as metal organic complexes but also as organic metal phosphate complexes. Also charcoal particles of polluted soils contain high amounts of heay metals. The accumulation affinity is quite similar to that of humic substances.